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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1974434Generated: November 1, 2026

Ethyl cyanoacetate → HCID 15219945, compound

https://huagongshe.com/reaction/1974434

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl cyanoacetateHCID 7764—
ReactantAmmonium AcetateHCID 517165—
Reactant2-anilinoacetophenoneHCID 1132624—
ProductHCID 15219945HCID 1521994535%

Reaction Conditions

Temperature180 °C

Reaction Steps

A mixture of 21.1 grams (0.1 mol) of 2-anilinoacetophenone, 31.8 grams (0.28 mol) of ethyl cyanoacetate, and 8 grams (0.13 mol) of ammonium acetate were placed in a reaction flask fitted with a distillation head. The reaction mixture was placed in an oil bath pre-heated to a temperature of 180° C. At a reaction temperature of 100° C. the solid mixture liquified and stirred easily. The internal temperature of the reaction rose to 150° C. over a period of 30 minutes while a colorless distillate was removed. After 30 minutes no further distillate was collected and the product mixture was cooled. To the dark homogeneous liquid product was added 40 mL of absolute ethanol with stirring. The precipitated yellow crystalline product was collected by filtration and washed with 3×10 mL ethanol, 2×25 mL ligroin, and air dried to afford 10.05 grams of crude product. Recrystallization from 80 mL of acetonitrile gave 9.1 grams (35 mmol, 35 % yield) of 3-cyano -1,4-diphenyl-3-pyrrolin-2-one as yellow crystals, m. p.=188°-190° C. Elemental Analysis: Calculated: C=78.44, H=4.65, N=10.76; Found: C=78.36, H=4.90, N=10.81.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05283165
Source datasetuspto-grants-1994_02
ORD IDord-8b94df35da7d452faffbdbcbb5a0a95d
Source noteuspto-grants-1994_02